Kanefron N - instructions for use, doses, side effects, contraindications

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Dosage form: & nbsppills

Composition:

For 1 pills:

Active components:
crushed medicinal plant raw materials:
A thousand acres of grass	18 mg
Lubistoca officinalis root	18 mg
Rosemary leaves	18 mg
Excipients:
Corn starch	15 mg
Silica colloidal dioxide	5.5 mg
Lactose Monohydrate	45.0 mg
Povidone	9.0 mg
Sheath:
Iron oxide red	0.049 mg
Riboflavin E 101	0.243 mg
Calcium carbonate	17.222 mg
Dextrose	0.972 mg
Corn starch	2,500 mg
Corn modified corn starch	2.140 mg
Wax mountain glycolic	0.075 mg
Povidone	0.103 mg
Castor oil	0.025 mg
Sucrose	57.182 mg
Shellac	0.615 mg
Talc	43.541 mg
Titanium dioxide	0.333 mg

Description:

Orange, round, biconvex dragee with a smooth surface.

Pharmacotherapeutic group:Diuretic remedy of plant origin

ATX: & nbsp

Other drugs for the treatment of urological diseases

Pharmacodynamics:

Combined preparation of plant origin, has a diuretic, antispasmodic, anti-inflammatory, antimicrobial effect.

Indications:

The drug is used in complex therapy for the treatment of chronic infections of the bladder (cystitis) and kidneys (pyelonephritis), with non-infectious chronic inflammation of the kidneys (glomerulonephritis, interstitial nephritis), as a remedy, preventing the formation of urinary stones (also after removal of urinary stones).

Contraindications:

Hypersensitivity to the components of the drug.

Children's age (up to 6 years).

Stomach ulcer and duodenal ulcer in the stage of exacerbation.

Insufficiency of lactase, lactose intolerance, glucose-galactose malabsorption.

Deficiency of sugar / isomaltase, intolerance to fructose.

Pregnancy and lactation:

The use of the drug during pregnancy and during breastfeeding is possible only according to the doctor's prescription, in strict accordance with the recommendations for use and after the assessment by the attending physician of the risk-benefit ratio.

Dosing and Administration:

Inside, not liquid, squeezed water.

Adults: 2 tablets 3 times a day.

Children school age: 1 tablet 3 times a day.

After weakening the severity of the disease The drug should be continued for 2-4 weeks.

During the treatment with the drug, consumption of a large amount of liquid is recommended.

Side effects:

Allergic reactions are possible.

Possible disorders of the gastrointestinal tract (nausea, vomiting, diarrhea).

If signs of an allergic reaction appear, stop taking the drug.

Overdose:

To date, data on overdose and intoxication are absent.

In case of an overdose of the drug, symptomatic treatment is prescribed.

Interaction:

Combination with antibacterial agents is possible and expedient.

Interactions with other drugs are currently unknown.

Special instructions:

When edema caused by impaired cardiac function or kidneys, the consumption of large amounts of fluid is contraindicated.

If the renal function is impaired, the drug should not be given as monotherapy.

In the case of inflammatory kidney disease, you should consult a doctor for advice.

In the case of blood in the urine, pain during urination, or with acute urinary retention, you should urgently consult a doctor.

The digestible carbohydrates contained in a single dragee are less than 0.04 "bread units" (XE).

Effect on the ability to drive transp. cf. and fur:

The drug does not affect the ability to perform potentially dangerous Activities requiring increased concentration of attention and speed psychomotor reactions (including the management of vehicles, work with moving mechanisms).

Form release / dosage:Dragee.

Packaging:

For 20 dragees in a blister of aluminum foil (bottom) and polyvinyl chloride / polyvinylidene chloride film (upper part).

For 3 or 6 blisters together with the instructions for use are placed in a folding cardboard box.

Storage conditions:

Store in a dry, dark place at a temperature of no higher than 25 ° C.

Keep out of the reach of children.

Shelf life:

3 years.

Do not use after the expiration date printed on the package.

Terms of leave from pharmacies:Without recipe

Registration number:П N014244 / 02

Date of registration:29.12.2011 / 19.10.2015

Expiration Date:Unlimited

The owner of the registration certificate:Bionoric CEBionoric CE Germany

Manufacturer: & nbsp

BIONORICA, SE Germany

Representation: & nbspBIONORIKA LLC BIONORIKA LLC Russia

Information update date: & nbsp30.11.2017

Illustrated instructions

Instructions

Kanefron® H (Canephron® N)